Evidence map›Paper›PMID 22096521›Full record

ArticlePloS one2011

Anti-transforming growth factor ß antibody treatment rescues bone loss and prevents breast cancer metastasis to bone.

Swati Biswas, Jeffry S Nyman, JoAnn Alvarez, Anwesa Chakrabarti, Austin Ayres, Julie Sterling, James Edwards, Tapasi Rana, Rachelle Johnson, Daniel S Perrien and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Article
  7. TGFβ1Nature communications · 2023
    Article
  8. The Osteoclast Traces the Route to Bone Tumors and Metastases.Frontiers in cell and developmental biology · 2022
    Review
  9. Article
  10. Review
  11. Review
  12. Biphasic α2β1 Integrin Expression in Breast Cancer Metastasis to Bone.International journal of molecular sciences · 2021
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 1 institution in 1 country.

Swati BiswasDepartment of Radiation Oncology, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America. swati.biswas@vanderbilt.edu
Jeffry S Nyman
JoAnn Alvarez
Anwesa Chakrabarti
Austin Ayres
Julie Sterling
James Edwards
Tapasi Rana
Rachelle Johnson
Daniel S Perrien
Scott Lonning
Yu Shyr
Lynn M Matrisian
Gregory R Mundy
Vanderbilt University · US

Funding

TUMORS EFFECTS ON THE SKELETONP01CA040035 · NCI · VANDERBILT UNIVERSITY · PI SUN, LUZHE · 1985 to 2010
$11.0M
MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
Protein Collection and Proteomics Integrative Shared ResourceU54CA126505 · NCI · VANDERBILT UNIVERSITY · PI MATRISIAN, LYNN M · 2006 to 2010
$8.2M
NCI NIH HHS P01 CA040035NCI NIH HHS T32 CA009592NCI NIH HHS U54 CA126505
6 · The paper itself

Abstract

Breast cancer often metastasizes to bone causing osteolytic bone resorption which releases active TGFβ. Because TGFβ favors progression of breast cancer metastasis to bone, we hypothesized that treatment using anti-TGFβ antibody may reduce tumor burden and rescue tumor-associated bone loss in metastatic breast cancer. In this study we have tested the efficacy of an anti-TGFβ antibody 1D11 preventing breast cancer bone metastasis. We have used two preclinical breast cancer bone metastasis models, in which either human breast cancer cells or murine mammary tumor cells were injected in host mice via left cardiac ventricle. Using several in vivo, in vitro and ex vivo assays, we have demonstrated that anti-TGFβ antibody treatment have significantly reduced tumor burden in the bone along with a statistically significant threefold reduction in osteolytic lesion number and tenfold reduction in osteolytic lesion area. A decrease in osteoclast numbers (p = 0.027) in vivo and osteoclastogenesis ex vivo were also observed. Most importantly, in tumor-bearing mice, anti-TGFβ treatment resulted in a twofold increase in bone volume (p<0.01). In addition, treatment with anti-TGFβ antibody increased the mineral-to-collagen ratio in vivo, a reflection of improved tissue level properties. Moreover, anti-TGFβ antibody directly increased mineralized matrix formation in calverial osteoblast (p = 0.005), suggesting a direct beneficial role of anti-TGFβ antibody treatment on osteoblasts. Data presented here demonstrate that anti-TGFβ treatment may offer a novel therapeutic option for tumor-induced bone disease and has the dual potential for simultaneously decreasing tumor burden and rescue bone loss in breast cancer to bone metastases. This approach of intervention has the potential to reduce skeletal related events (SREs) in breast cancer survivors.

Indexed as

AnimalsAntibodiesBone and BonesBone NeoplasmsBreast NeoplasmsCell DifferentiationCell Line, TumorCollagenFemaleHumansMiceMice, NudeOsteoblastsOsteoclastsOsteogenesisReal-Time Polymerase Chain ReactionAntibodiesCollagenTransforming Growth Factor beta

Identifiers

PMID22096521
PMCPMC3214031
OpenAlexW2087653913

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.